Difference between revisions of "Master Regulator Analysis"

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==Overview==
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The Master Regulator Analysis (MRA) component works with a microarray gene expression dataset.
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Its goal is to identify transcription factors (TFs) which control the regulation of a set of target genes (TGs) that demonstrate significant differential expression.  Differential expression is measured using a simple t-test across 2 cellular phenotypes, e.g. “Case” and “Control”.
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The types of data which will be used are:
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# The results of a t-test for differential expression on the selected microarray dataset.
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# A list of putative transcription factors which are to be tested against the differentially expressed genes.
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# An interaction network in the form of an ARACNe adjacency matrix.  It should contain the results of an ARACNe run including, as hub markers, at least all of the transcription factors listed above, and computed against the markers (dataset) to be tested for differential expression.
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Briefly, the steps which MRA will execute are:
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# Run a t-test on the the microarray dataset selected in the Project Folders component.
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# For each TF, the set of its nearest neighbors (in the adjacency matrix), that is, those markers showing the closest interaction with it, are tested for overlap with the set of differentially expressed genes using Fisher's Exact test.
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# The result is a list of transcription factors whose interactions show a significant overlap with the differentially expressed genes.
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==Parameters and Settings==
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===Load Network===
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* From File
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* From Network
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===Transcription Factors===
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* From File
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* From Sets
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===Significance Treshold===
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* T-test p-value (alpha)
  
  

Revision as of 17:54, 14 July 2009

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Overview

The Master Regulator Analysis (MRA) component works with a microarray gene expression dataset. Its goal is to identify transcription factors (TFs) which control the regulation of a set of target genes (TGs) that demonstrate significant differential expression. Differential expression is measured using a simple t-test across 2 cellular phenotypes, e.g. “Case” and “Control”.

The types of data which will be used are:

  1. The results of a t-test for differential expression on the selected microarray dataset.
  2. A list of putative transcription factors which are to be tested against the differentially expressed genes.
  3. An interaction network in the form of an ARACNe adjacency matrix. It should contain the results of an ARACNe run including, as hub markers, at least all of the transcription factors listed above, and computed against the markers (dataset) to be tested for differential expression.


Briefly, the steps which MRA will execute are:

  1. Run a t-test on the the microarray dataset selected in the Project Folders component.
  2. For each TF, the set of its nearest neighbors (in the adjacency matrix), that is, those markers showing the closest interaction with it, are tested for overlap with the set of differentially expressed genes using Fisher's Exact test.
  3. The result is a list of transcription factors whose interactions show a significant overlap with the differentially expressed genes.

Parameters and Settings

Load Network

  • From File
  • From Network

Transcription Factors

  • From File
  • From Sets

Significance Treshold

  • T-test p-value (alpha)


T MRA Setup.png


T MRA t-test.png